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Snorestop Nux vomica, Belladonna, Hydrastis canadensis, Kali bichromicum, Teucrium marum, Histaminum hydrochloricum, Laurocerasus, Cinchona, Stramonium 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X Spray, 59 mL

by Green Pharmaceuticals Inc · 59 mL in 1 BOTTLE, SPRAY (61152-600-59)
NDC 61152-0600-59
🏷️ FDA NDC (as labeled) 61152-600-59 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 61152-600-59
Product NDC 61152-600
11-digit billing NDC 61152060059
UNII F26P2D4757, 292E43P4I9, 269XH13919, R763EBH88T, WQZ3G9PF0H, 3POA0Q644U +3 more
SPL Set ID 37f4ea81-691f-597b-e063-6294a90a84bd
Established class (EPC) Non-Standardized Plant Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Plant Proteins; Seed Storage Proteins
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-06-19
Route ORAL
Dosage form SPRAY
Substance PRUNUS LAUROCERASUS LEAF; CINCHONA BARK; STRYCHNOS NUX-VOMICA SEED; HYDRASTIS CANADENSIS WHOLE; ATROPA BELLADONNA; HISTAMINE DIHYDROCHLORIDE; TEUCRIUM MARUM; DATURA STRAMONIUM; POTASSIUM DICHROMATE
Why two NDCs? The FDA registers this code as 61152-600-59 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 61152-0600-59. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerGreen Pharmaceuticals Inc
Labeler code61152
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio5 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

Snorestop is an unapproved homeopathic oral spray containing nine plant and mineral substances. In homeopathic practice, these ingredients are traditionally used to address snoring and related breathing concerns during sleep. Homeopathic products are marketed based on traditional use rather than FDA evaluation for effectiveness. The ingredients include botanical extracts like nux vomica, belladonna, and stramonium, along with mineral salts and other plant materials prepared according to homeopathic methods.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

3 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesCitric Acid Potassium Sorbate USP Purified Water

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Snorestop 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_Xthis 61152-0600-59 Green 59 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2025
On the market since
Jun 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Snorestop (this brand).

Top reported reactions

Dizziness1
Pruritus1
Rash Macular1
Wrong Technique In Drug Usage Process1

Reporter sex

2 reports
Female · 100%
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
61152-0600-59 You're viewing this 59 mL in 1 BOTTLE, SPRAY (61152-600-59) 2025-06-19 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Snorestop Nux vomica, Belladonna, Hydrastis canadensis, Kali bichromicum, Teucrium marum, Histaminum hydrochloricum, Laurocerasus, Cinchona, Stramonium 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X SPRAY is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 61152-600-59, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 61152-0600-59, written without dashes as 61152060059. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 61152-0600-59, the first segment (61152) is the labeler code FDA assigned to Green Pharmaceuticals Inc; the middle segment (0600) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (59) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Green Pharmaceuticals Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Green Pharmaceuticals Inc is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 11 words ▾

Uses: Temporarily relieves symptoms of non-apneic snoring. Individual results may vary.

⏱️ Dosage and Administration 72 words ▾

Directions: Adults and children 12 years of age and older: Spray twice under the tongue and twice in the back of the throat at bedtime. Use 30 mins apart from any food, water, or medicine. Initially, depress pump until primed. Please allow 3-5 days for initial treatment. Consult a physician for use in children under 12 years of age. Use additionally as needed, up to 4 times per day. Dosage and Administration

⚠️ Warnings 60 words ▾

Warnings: Use only as directed. Keep out of reach of children. Do not use on children under 12 years of age. This product does not treat sleep apnea. If you have sleep apnea,consult a health professional. If pregnant or breastfeeding, ask a health professional before use. Stop use and ask a doctor if symptoms do not improve in 7 days.

📦 Storage and Handling 14 words ▾

Other information Tamper resistant for your protection. Use only if safety seal is intact.

🧪 Active Ingredient 63 words ▾

Ingredients (HPUS): Equal volumes of each HPUS ingredient in 10X, 30X. Nux vomica 10X, 20X, & 30X, Belladonna 10X, 20X, & 30X, Hydrastis canadensis 10X, 20X, & 30X, Kali bichromicum 10X, 20X, & 30X, Teucrium marum 10X, 20X, & 30X, Histaminum hydrochloricum 10X, 20X, & 30X, Laurocerasus 10X, 20X, & 30X, Cinchona10X, 20X, & 30X, Stramonium 10X, 20X, & 30X. Snorestop Oral Spray

🧪 Inactive Ingredients 9 words ▾

Inactive Ingredients: Citric Acid Potassium Sorbate USP Purified Water

🎯 Purpose 14 words ▾

Purpose: Temporarily helps stop or reduce symptoms of non-apneic snoring. Individual results may vary.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 61152-0400-15 · Green 61152-0601-59 · Green →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.